Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof

ABSTRACT

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present invention concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer&#39;s disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases due to mutations in Wnt signaling components. Also provided are methods for treating Wnt-related disease states.

RELATED APPLICATIONS Cross-Reference to Related Applications

This application is a continuation application of U.S. application Ser. No. 13/552,188, filed Jul. 18, 2012, which is a continuation of U.S. application Ser. No. 12/852,706, filed Aug. 9, 2010, which claims the benefit of U.S. Provisional Application No. 61/232,603, filed Aug. 10, 2009 and U.S. Provisional Application No. 61/305,459, filed Feb. 17, 2010, all of which are incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to inhibitors of one or more proteins in the Wnt pathway, including inhibitors of one or more Wnt proteins, and compositions comprising the same. More particularly, it concerns the use of an indazole compound or salts or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases due to mutations in Wnt signaling components.

2. Description of the Related Art

Pattern formation is the activity by which embryonic cells form ordered spatial arrangements of differentiated tissues. Speculation on the mechanisms underlying these patterning effects usually centers on the secretion of a signaling molecule that elicits an appropriate response from the tissues being patterned. More recent work aimed at the identification of such signaling molecules implicates secreted proteins encoded by individual members of a small number of gene families.

A longstanding idea in cancer biology is that cancers arise and grow due to the formation of cancer stem cells, which may constitute only a minority of the cells within a tumor but are nevertheless critical for its propagation. Stem cells are appealing as the cell of origin for cancer because of their pre-existing capacity for self-renewal and for unlimited replication. In addition, stem cells are relatively long-lived in comparison to other cells within tissues, providing a greater opportunity to accumulate the multiple additional mutations that may be required to increase the rate of cell proliferation and produce clinically significant cancers. Of particular recent interest in the origin of cancer is the observation that the Wnt signaling pathway, which has been implicated in stem cell self-renewal in normal tissues, upon continuous activation has also been associated with the initiation and growth of many types of cancer. This pathway thus provides a potential link between the normal self-renewal of stem cells and the aberrantly regulated proliferation of cancer stem cells.

The Wnt growth factor family includes more than 10 genes identified in the mouse and at least 7 genes identified in the human. Members of the Wnt family of signaling molecules mediate many important short- and long-range patterning processes during invertebrate and vertebrate development. The Wnt signaling pathway is known for its important role in the inductive interactions that regulate growth and differentiation, and likely also plays important roles in the homeostatic maintenance of post-embryonic tissue integrity. Wnt stabilizes cytoplasmic p-catenin, which stimulates the expression of genes including c-myc, c jun, fra-1, and cyclin D1. In addition, misregulation of Wnt signaling can cause developmental defects and is implicated in the genesis of several human cancers. More recently, the Wnt pathway has been implicated in the maintenance of stem or progenitor cells in a growing list of adult tissues that now includes skin, blood, gut, prostate, muscle and the nervous system.

Pathological activation of the Wnt pathway is also believed to be the initial event leading to colorectal cancer in over 85% of all sporadic cases in the Western world. Activation of the Wnt pathway has also been extensively reported for hepatocellular carcinoma, breast cancer, ovarian cancer, pancreatic cancer, melanomas, mesotheliomas, lymphomas and leukemias. In addition to cancer, inhibitors of the Wnt pathway can be used for stem cell research or for the treatment of any diseases characterized by aberrant Wnt activation such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, psoriasis as well as mycotic and viral infections and bone and cartilage diseases. As such, it is a therapeutic target that is of great interest to the field.

In addition to cancer, there are many cases of genetic diseases due to mutations in Wnt signaling components. Examples of some of the many diseases are Alzheimer's disease [Proc. Natl. Acad. Sci. USA (2007), 104(22), 9434-9], osteoarthritis, polyposis coli [Science (1991), 253(5020), 665-669], osteoporosis-pseudoglioma syndrome [N. Engl. J. Med. (2002), 346(20), 1513-21], familial exudative vitreoretinopathy [Hum. Mutat. (2005), 26(2), 104-12], retinal angiogenesis [Nat. Genet. (2002), 32(2), 326-30], early coronary disease [Science (2007), 315(5816), 1278-82], tetra-amelia syndrome [Am. J. Hum. Genet. (2004), 74(3), 558-63], Müllerian-duct regression and virilization [Engl. J. Med (2004), 351(8), 792-8], SERKAL syndrome [Am. J. Hum. Genet. (2008), 82(1), 39-47], diabetes mellitus type 2 [Am. J. Hum. Genet. (2004), 75(5), 832-43; N. Engl. J. Med (2006), 355(3), 241-50], Fuhrmann syndrome [Am. J. Hum. Genet. (2006), 79(2), 402-8], Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome [Am. J. Hum. Genet. (2006), 79(2), 402-8], odonto-onycho-dermal dysplasia [Am. J. Hum. Genet. (2007), 81(4), 821-8], obesity [Diabetologia (2006), 49(4), 678-84], split-hand/foot malformation [Hum. Mol. Genet. (2008), 17(17), 2644-53], caudal duplication syndrome [Am. J. Hum. Genet. (2006), 79(1), 155-62], tooth agenesis [Am. J. Hum. Genet. (2004), 74(5), 1043-50], Wilms tumor [Science (2007), 315(5812), 642-5], skeletal dysplasia [Nat. Genet. (2009), 41(1), 95-100], focal dermal hypoplasia [Nat. Genet. (2007), 39(7), 836-8], autosomal recessive anonychia [Nat. Genet. (2006), 38(11), 1245-7], neural tube defects [N. Engl. J. Med (2007), 356(14), 1432-7], alpha-thalassemia (ATRX) syndrome [The Journal of Neuroscience (2008), 28(47), 12570-12580], fragile X syndrome [PLoS Genetics (2010), 6(4), e1000898], ICF syndrome, Angelman syndrome [Brain Research Bulletin (2002), 57(1), 109-119], Prader-Willi syndrome [Journal of Neuroscience (2006), 26(20), 5383-5392], Beckwith-Wiedemann Syndrome [Pediatric and Developmental Pathology (2003), 6(4), 299-306] and Rett syndrome.

SUMMARY OF THE INVENTION

The present invention makes available methods and reagents, involving contacting a cell with an agent, such as an aromatic compound, in a sufficient amount to antagonize a Wnt activity, e.g., to reverse or control an aberrant growth state or correct an genetic disorder due to mutations in Wnt signaling components.

Some embodiments disclosed herein include Wnt inhibitors containing an indazole core. Other embodiments disclosed herein include pharmaceutical compositions and methods of treatment using these compounds.

One embodiment disclosed herein includes a compound having the structure of formula I:

as well as prodrugs and pharmaceutically acceptable salts thereof.

In some embodiments of formula (I):

R¹, R², R⁴, R⁶, R⁷, R⁸ and R⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰), —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)NR¹⁰C(═O)OR¹⁰, —(C₁₋₉ alkyl)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)N(R¹⁰)C(=A)R¹⁰, —(C₁₋₉ alkyl)_(n)OC(═O)N(R¹⁰)₂, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)C(=A)R¹⁰;

R³ is selected from the group consisting of —NRS(═O)R¹⁴, —(C₁₋₉ alkyl)R¹⁴, -carbocyclylR¹⁴R¹⁵, -heterocyclylR¹⁴R¹⁵, -arylR¹⁴R¹⁵ or -heteroarylR¹⁴R¹⁵;

alternatively, one of each R¹ and R², R² and R³, R³ and R⁴, R⁶ and R⁷, R⁷ and R⁸ or R⁸ and R⁹ are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl,

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond;

each R¹⁰ is independently selected from the group consisting of H, —C₁₋₄ alkyl, —CF₃, —(C₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl;

each R¹¹ is independently selected from the group consisting of —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl;

each R¹² is independently selected from the group consisting of CN, —OR¹⁰ and R¹⁰;

R¹³ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹³, heterocyclylR¹³, arylR¹³, heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)NR¹⁰C(═O)OR¹⁰, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰), —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —(C₁₋₉ alkyl)_(n)OC(═O)N(R¹⁰)₂, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰;

R¹⁴ is selected from the group consisting of —NR¹⁰C(=A)R, —NR¹⁰S(═O)R¹¹, —NR¹⁰SO₂R¹⁰, —NR¹⁰C(═O)N(R¹⁶)₂, —NR¹⁰C(═S)N(R¹⁰)₂, —NR¹⁰C(═NR¹²)N(R¹⁰)₂, N(R¹⁶)₂, —C(═O)NR¹⁰R¹⁷, —C(═S)N(R¹⁰)₂, —C(═NR¹²)N(R¹⁰)₂, —OC(=A)R¹⁰, —C(=A)R¹⁰, —NR¹⁰C(=A)OR¹⁰ and —OC(=A)NR¹⁰R¹⁰;

R¹⁵ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹³, heterocyclylR³, arylR¹³, heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₄ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)NR¹⁰C(═O)OR¹⁰, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —(C₁₋₉ alkyl)_(n)OC(═O)N(R¹⁰)₂, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰;

R¹⁶ is —C₁₋₉ alkyl;

each R¹⁷ is independently selected from the group consisting of -heterocyclylR¹³, —(C₁₋₉ alkyl)heterocyclylR¹³ and —(C₁₋₉ alkyl)carbocyclylR³;

R¹⁸ and R¹⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —(C₁₋₉ alkyl)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)arylR¹³, —(C₁₋₉ alkyl)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)SR¹⁰, —(C₁₋₉ alkyl)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)N(RO)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰;

alternatively, R¹⁸ and R¹⁹ are taken together to form a ring which is selected from the group consisting of benzene and pyridine;

each A is independently selected from O, S and NR¹²;

X is nitrogen and R⁵ is absent;

Y¹, Y², Y³ and Y⁴ are independently selected from the group consisting of carbon and nitrogen with the proviso that at least one of Y¹, Y², Y³ and Y⁴ are nitrogen;

if Y¹ is nitrogen then R⁶ is absent;

if Y² is nitrogen then R⁷ is absent;

if Y³ is nitrogen then R⁸ is absent;

if Y⁴ is nitrogen then R⁹ is absent; and

each n is 0 or 1.

In other embodiments of formula (I):

R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸ and R⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, —(C₁₋₉ alkyl)carbocyclylR¹², —(C₁₋₉ alkyl)_(n)heterocyclylR¹², —(C₁₋₉ alkyl)_(n)arylR¹², —(C₁₋₉ alkyl)_(n)heteroarylR¹², —(C₁₋₉ alkyl)OR⁹, —(C₁₋₉ alkyl)_(n)SR⁹, —(C₁₋₉ alkyl)S(═O)R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂R⁹, —(C₁₋₉ alkyl)_(n)N(R⁹)S(═O)R¹⁰, —(C₁₋₉ alkyl)_(n)N(R⁹)SO₂R⁹, —(C₁₋₉ alkyl)_(n)SO₂N(R⁹)₂, —(C₁₋₉ alkyl)_(n)N(R⁹)₂, —(C₁₋₉ alkyl)_(n)N(R⁹)C(=A)N(R⁹)₂, —(C₁₋₉ alkyl)NR⁹C(═O)OR⁹, —(C₁₋₉ alkyl)_(n)C(=A)N(R⁹)₂, —(C₁₋₉ alkyl)N(R⁹)C(=A)R⁹, —(C₁₋₉ alkyl)_(n)OC(═O)NR⁹R⁹, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R⁹ and —(C₁₋₉ alkyl)_(n)C(=A)R⁹;

alternatively, one of each R¹ and R², R² and R³, R³ and R⁴, R⁶ and R⁷, R⁷ and R⁸ or R⁸ and R⁹ are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl,

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond;

each R¹⁰ is independently selected from the group consisting of H, —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl;

each R¹¹ is independently selected from the group consisting of —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl;

each R¹² is independently selected from the group consisting of CN, —OR¹⁰ and R¹⁰;

R¹³ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹², heterocyclylR², arylR¹², heteroarylR¹², —(C₁₋₉ alkyl)_(n)OR⁹, —(C₁₋₉ alkyl)_(n)SR⁹, —(C₁₋₉ alkyl)_(n)S(═O)R⁹, —(C₁₋₉ alkyl)_(n)SO₂R⁹, —(C₁₋₉ alkyl)_(n)N(R⁹)SO₂R⁹, —(C₁₋₉ alkyl)_(n)SO₂N(R⁹)₂, —(C₁₋₉ alkyl)_(n)N(R⁹)₂, —(C₁₋₉ alkyl)_(n)N(R⁹)C(=A)N(R⁹)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R⁹)₂, —(C₁₋₉ alkyl)_(n)NR⁹C(O)OR⁹, —(C₁₋₉ alkyl)_(n)N(R⁹)C(=A)R⁹, —(C₁₋₉ alkyl)_(n)OC(═O)N(R⁹)₂, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R⁹ and —(C₁₋₉ alkyl)_(n)C(=A)R⁹;

R¹⁸ and R¹⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰;

alternatively, R¹⁸ and R¹⁹ are taken together to form a ring which is selected from the group consisting of benzene and pyridine;

each A is independently selected from O, S and NR¹²;

X is carbon;

Y¹, Y², Y³ and Y⁴ are independently selected from the group consisting of carbon and nitrogen with the proviso that at least one of Y¹, Y², Y³ and Y⁴ are nitrogen;

if Y¹ is nitrogen then R⁶ is absent;

if Y² is nitrogen then R⁷ is absent;

if Y³ is nitrogen then R⁸ is absent;

if Y⁴ is nitrogen then R⁹ is absent; and

each n is 0 or 1, or a pharmaceutically acceptable salt or pro-drug thereof.

Some embodiments include stereoisomers and pharmaceutically acceptable salts of a compound of general formula (I).

Some embodiments include pro-drugs of a compound of general formula (I).

Some embodiments of the present invention include pharmaceutical compositions comprising a compound of general formula (I) and a pharmaceutically acceptable carrier.

Other embodiments disclosed herein include methods of inhibiting one or more members of the Wnt pathway, including one or more Wnt proteins by administering to a subject affected by a disorder or disease in which aberrant Wnt signaling is implicated, such as cancer and other diseases associated with abnormal angiogenesis, cellular proliferation, cell cycling and mutations in Wnt signaling components, a compound according to any of the above formulas. Accordingly, the compounds and compositions provided herein can be used to treat cancer, to reduce or inhibit angiogenesis, to reduce or inhibit cellular proliferation and correct an genetic disorder due to mutations in Wnt signaling components. Non-limiting examples of diseases which can be treated with the compounds and compositions provided herein include a variety of cancers, diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, psoriasis, mycotic and viral infections, osteochondrodysplasia, Alzheimer's disease, osteoarthritis, polyposis coli, osteoporosis-pseudoglioma syndrome, familial exudative vitreoretinopathy, retinal angiogenesis, early coronary disease, tetra-amelia syndrome, Müllerian-duct regression and virilization, SERKAL syndrome, diabetes mellitus type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity, split-hand/foot malformation, caudal duplication syndrome, tooth agenesis, Wilms tumor, skeletal dysplasia, focal dermal hypoplasia, autosomal recessive anonychia, neural tube defects, alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF syndrome, Angelman syndrome, Prader-Willi syndrome, Beckwith-Wiedemann Syndrome and Rett syndrome.

Another embodiment disclosed herein includes a pharmaceutical composition that has a compound according to any of the above formulas and a pharmaceutically acceptable carrier, diluent, or excipient.

Some embodiments of the present invention include methods to prepare a compound of general formula (I).

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.

DETAILED DESCRIPTION OF THE INVENTION

Compositions and methods for inhibiting one or more members of the Wnt pathway, including one or more Wnt proteins would be of tremendous benefit. Certain embodiments provide such compositions and methods.

Some embodiments relate to a method for treating a disease such as cancers, diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, psoriasis, mycotic and viral infections, osteochondrodysplasia, Alzheimer's disease, osteoarthritis, polyposis coli, osteoporosis-pseudoglioma syndrome, familial exudative vitreoretinopathy, retinal angiogenesis, early coronary disease, tetra-amelia syndrome, Müllerian-duct regression and virilization, SERKAL syndrome, diabetes mellitus type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity, split-hand/foot malformation, caudal duplication syndrome, tooth agenesis, Wilms tumor, skeletal dysplasia, focal dermal hypoplasia, autosomal recessive anonychia, neural tube defects, alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF syndrome, Angelman syndrome, Prader-Willi syndrome, Beckwith-Wiedemann Syndrome and Rett syndrome.

In some embodiments, pharmaceutical compositions are provided that are effective for treatment of a disease of an animal, e.g., a mammal, caused by the pathological activation or mutations of the Wnt pathway. The composition includes a pharmaceutically acceptable carrier and a Wnt pathway inhibitor as described herein.

DEFINITIONS

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art to which this disclosure belongs. All patents, applications, published applications, and other publications are incorporated by reference in their entirety. In the event that there is a plurality of definitions for a term herein, those in this section prevail unless stated otherwise.

In this specification and in the claims, the following terms have the meanings as defined. As used herein, “alkyl” means a branched, or straight chain chemical group containing only carbon and hydrogen, such as methyl, isopropyl, isobutyl, sec-butyl and pentyl. Alkyl groups can either be unsubstituted or substituted with one or more substituents, e.g., halogen, alkoxy, acyloxy, amino, amido, cyano, nitro, hydroxyl, mercapto, carboxy, carbonyl, benzyloxy, aryl, heteroaryl, or other functionality that may be suitably blocked, if necessary for purposes of the invention, with a protecting group. Alkyl groups can be saturated or unsaturated (e.g., containing —C═C— or —C≡C— subunits), at one or several positions. Typically, alkyl groups will comprise 1 to 9 carbon atoms, preferably 1 to 6, and more preferably 1 to 4 carbon atoms.

As used herein, “carbocyclyl” means a cyclic ring system containing only carbon atoms in the ring system backbone, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cyclohexenyl. Carbocyclyls may include multiple fused rings. Carbocyclyls may have any degree of saturation provided that at least one ring in the ring system is not aromatic. Carbocyclyl groups can either be unsubstituted or substituted with one or more substituents, e.g., halogen, alkoxy, acyloxy, amino, amido, cyano, nitro, hydroxyl, mercapto, carboxy, carbonyl, benzyloxy, aryl, heteroaryl, or other functionality that may be suitably blocked, if necessary for purposes of the invention, with a protecting group. Typically, carbocyclyl groups will comprise 3 to 10 carbon atoms, preferably 3 to 6.

As used herein, “lower alkyl” means a subset of alkyl, and thus is a hydrocarbon substituent, which is linear, or branched. Preferred lower alkyls are of 1 to about 4 carbons, and may be branched or linear. Examples of lower alkyl include butyl, propyl, isopropyl, ethyl, and methyl. Likewise, radicals using the terminology “lower” refer to radicals preferably with 1 to about 4 carbons in the alkyl portion of the radical.

As used herein, “amido” means a H—CON— or alkyl-CON—, carbocyclyl-CON—, aryl-CON—, heteroaryl-CON— or heterocyclyl-CON group wherein the alkyl, carbocyclyl, aryl or heterocyclyl group is as herein described.

As used herein, “aryl” means an aromatic radical having a single-ring (e.g., phenyl) or multiple condensed rings (e.g., naphthyl or anthryl) with only carbon atoms present in the ring backbone. Aryl groups can either be unsubstituted or substituted with one or more substituents, e.g., amino, cyano, hydroxyl, lower alkyl, haloalkyl, alkoxy, nitro, halo, mercapto, and other substituents. A preferred carbocyclic aryl is phenyl.

As used herein, the term “heteroaryl” means an aromatic radical having one or more heteroatom(s) (e.g., N, O, or S) in the ring backbone and may include a single ring (e.g., pyridine) or multiple condensed rings (e.g., quinoline). Heteroaryl groups can either be unsubstituted or substituted with one or more substituents, e.g., amino, cyano, hydroxyl, lower alkyl, haloalkyl, alkoxy, nitro, halo, mercapto, and other substituents. Examples of heteroaryl include thienyl, pyrridyl, furyl, oxazolyl, oxadiazolyl, pyrollyl, imidazolyl, triazolyl, thiodiazolyl, pyrazolyl, isoxazolyl, thiadiazolyl, pyranyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, thiazolyl and others.

In these definitions it is clearly contemplated that substitution on the aryl and heteroaryl rings is within the scope of certain embodiments. Where substitution occurs, the radical is called substituted aryl or substituted heteroaryl. Preferably one to three and more preferably one or two substituents occur on the aryl ring. Though many substituents will be useful, preferred substituents include those commonly found in aryl compounds, such as alkyl, cycloalkyl, hydroxy, alkoxy, cyano, halo, haloalkyl, mercapto and the like.

As used herein, “amide” includes both RNR′CO— (in the case of R=alkyl, alkaminocarbonyl-) and RCONR′— (in the case of R=alkyl, alkyl carbonylamino-).

As used herein, the term “ester” includes both ROCO— (in the case of R=alkyl, alkoxycarbonyl-) and RCOO— (in the case of R=alkyl, alkylcarbonyloxy-).

As used herein, “acyl” means an H—CO— or alkyl-CO—, carbocyclyl-CO—, aryl-CO—, heteroaryl-CO— or heterocyclyl-CO— group wherein the alkyl, carbocyclyl, aryl or heterocyclyl group is as herein described. Preferred acyls contain a lower alkyl. Exemplary alkyl acyl groups include formyl, acetyl, propanoyl, 2-methylpropanoyl, t-butylacetyl, butanoyl and palmitoyl.

As used herein, “halo or halide” is a chloro, bromo, fluoro or iodo atom radical. Chloro, bromo and fluoro are preferred halides. The term “halo” also contemplates terms sometimes referred to as “halogen”, or “halide”.

As used herein, “haloalkyl” means a hydrocarbon substituent, which is linear or branched or cyclic alkyl, alkenyl or alkynyl substituted with chloro, bromo, fluoro or iodo atom(s). Most preferred of these are fluoroalkyls, wherein one or more of the hydrogen atoms have been substituted by fluoro. Preferred haloalkyls are of 1 to about 3 carbons in length, more preferred haloalkyls are 1 to about 2 carbons, and most preferred are 1 carbon in length. The skilled artisan will recognize then that as used herein, “haloalkylene” means a diradical variant of haloalkyl, such diradicals may act as spacers between radicals, other atoms, or between the parent ring and another functional group.

As used herein, “heterocyclyl” means a cyclic ring system comprising at least one heteroatom in the ring system backbone. Heterocyclyls may include multiple fused rings. Heterocyclyls may have any degree of saturation provided that at least one ring in the ring system is not aromatic. Heterocyclyls may be substituted or unsubstituted with one or more substituents, e.g., halogen, alkoxy, acyloxy, amino, amido, cyano, nitro, hydroxyl, mercapto, carboxy, carbonyl, benzyloxy, aryl, heteroaryl, and other substituents, and are attached to other groups via any available valence, preferably any available carbon or nitrogen. More preferred heterocycles are of 5-7 members. In six membered monocyclic heterocycles, the heteroatom(s) are selected from one up to three of O, N or S, and wherein when the heterocycle is five membered, preferably it has one or two heteroatoms selected from O, N, or S.

As used herein, “substituted amino” means an amino radical which is substituted by one or two alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl groups, wherein the alkyl, aryl, heteroaryl or heterocyclyl are defined as above.

As used herein, “substituted thiol” means RS— group wherein R is an alkyl, an aryl, heteroaryl or a heterocyclyl group, wherein the alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl are defined as above.

As used herein, “sulfonyl” means an alkylSO₂, arylSO₂, heteroarylSO₂, carbocyclylSO₂, or heterocyclyl-SO₂ group wherein the alkyl, carbocyclyl, aryl, heteroaryl or heterocyclyl are defined as above.

As used herein, “sulfamido” means an alkyl-N—S(O)₂N—, aryl-NS(O)₂N—, heteroaryl-NS(O)₂N—, carbocyclyl-NS(O)₂N or heterocyclyl-NS(O)₂N— group wherein the alkyl, carbocyclyl, aryl, heteroaryl or heterocyclyl group is as herein described.

As used herein, “sulfonamido” means an alkyl-S(O)₂N—, aryl-S(O)₂N—, heteroaryl-S(O)₂N—, carbocyclyl-S(O)₂N— or heterocyclyl-S(O)₂N— group wherein the alkyl, carbocyclyl, aryl, heteroaryl or heterocyclyl group is as herein described.

As used herein, “ureido” means an alkyl-NCON—, aryl-NCON—, heteroaryl-NCON—, carbocyclyl-NCON— or heterocyclyl-NCON— group wherein the alkyl, carbocyclyl, aryl, heteroaryl or heterocyclyl group is as herein described.

As used herein, when two groups are indicated to be “linked” or “bonded” to form a “ring,” it is to be understood that a bond is formed between the two groups and may involve replacement of a hydrogen atom on one or both groups with the bond, thereby forming a carbocyclyl, heterocyclyl, aryl, or heteroaryl ring. The skilled artisan will recognize that such rings can and are readily formed by routine chemical reactions, and it is within the purview of the skilled artisan to both envision such rings and the methods of their formations. Preferred are rings having from 3-7 members, more preferably 5 or 6 members. As used herein the term “ring” or “rings” when formed by the combination of two radicals refers to heterocyclic, carbocyclic, aryl, or heteroaryl rings.

The skilled artisan will recognize that some structures described herein may be resonance forms or tautomers of compounds that may be fairly represented by other chemical structures, even when kinetically, the artisan recognizes that such structures are only a very small portion of a sample of such compound(s). Such compounds are clearly contemplated within the scope of this invention, though such resonance forms or tautomers are not represented herein.

The compounds provided herein may encompass various stereochemical forms. The compounds also encompasses diastereomers as well as optical isomers, e.g. mixtures of enantiomers including racemic mixtures, as well as individual enantiomers and diastereomers, which arise as a consequence of structural asymmetry in certain compounds. Separation of the individual isomers or selective synthesis of the individual isomers is accomplished by application of various methods which are well known to practitioners in the art. Unless otherwise indicated, when a disclosed compound is named or depicted by a structure without specifying the stereochemistry and has one or more chiral centers, it is understood to represent all possible stereoisomers of the compound.

The term “administration” or “administering” refers to a method of giving a dosage of a compound or pharmaceutical composition to a vertebrate or invertebrate, including a mammal, a bird, a fish, or an amphibian, where the method is, e.g., intrarespiratory, topical, oral, intravenous, intraperitoneal, intramuscular, buccal, rectal, sublingual. The preferred method of administration can vary depending on various factors, e.g., the components of the pharmaceutical composition, the site of the disease, the disease involved, and the severity of the disease.

A “diagnostic” as used herein is a compound, method, system, or device that assists in the identification and characterization of a health or disease state. The diagnostic can be used in standard assays as is known in the art.

The term “mammal” is used in its usual biological sense. Thus, it specifically includes humans, cattle, horses, dogs, and cats, but also includes many other species.

The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable excipient” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions. In addition, various adjuvants such as are commonly used in the art may be included. These and other such compounds are described in the literature, e.g., in the Merck Index, Merck & Company, Rahway, N.J. Considerations for the inclusion of various components in pharmaceutical compositions are described, e.g., in Gilman et al. (Eds.) (2006); Goodman and Gilman's: The Pharmacological Basis of Therapeutics, 11th Ed., The McGraw-Hill Companies.

The term “pharmaceutically acceptable salt” refers to salts that retain the biological effectiveness and properties of the compounds of the preferred embodiments and, which are not biologically or otherwise undesirable. In many cases, the compounds of the preferred embodiments are capable of forming acid and/or base salts by virtue of the presence of amino and/or carboxyl groups or groups similar thereto. Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids. Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like. Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, and the like. Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases. Inorganic bases from which salts can be derived include, for example, sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum, and the like; particularly preferred are the ammonium, potassium, sodium, calcium and magnesium salts. Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines, basic ion exchange resins, and the like, specifically such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, and ethanolamine. Many such salts are known in the art, as described in World Patent Publication 87/05297, Johnston et al., published Sep. 11, 1987 (incorporated by reference herein).

“Solvate” refers to the compound formed by the interaction of a solvent and a Wnt pathway inhibitor, a metabolite, or salt thereof. Suitable solvates are pharmaceutically acceptable solvates including hydrates.

“Subject” as used herein, means a human or a non-human mammal, e.g., a dog, a cat, a mouse, a rat, a cow, a sheep, a pig, a goat, a non-human primate or a bird, e.g., a chicken, as well as any other vertebrate or invertebrate.

By “therapeutically effective amount” or “pharmaceutically effective amount” is typically one which is sufficient to achieve the desired effect and may vary according to the nature and severity of the disease condition, and the potency of the compound. It will be appreciated that different concentrations may be employed for prophylaxis than for treatment of an active disease. This amount can further depend upon the patient's height, weight, sex, age and medical history.

A therapeutic effect relieves, to some extent, one or more of the symptoms of the disease, and includes curing a disease. “Curing” means that the symptoms of active disease are eliminated. However, certain long-term or permanent effects of the disease may exist even after a cure is obtained (such as extensive tissue damage).

“Treat,” “treatment,” or “treating,” as used herein refers to administering a pharmaceutical composition for therapeutic purposes. The term “therapeutic treatment” refers to administering treatment to a patient already suffering from a disease thus causing a therapeutically beneficial effect, such as ameliorating existing symptoms, preventing additional symptoms, ameliorating or preventing the underlying metabolic causes of symptoms, postponing or preventing the further development of a disorder and/or reducing the severity of symptoms that will or are expected to develop.

Compounds

The compounds and compositions described herein can be used as anti-proliferative agents, e.g., anti-cancer and anti-angiogenesis agents, and as inhibitors of the Wnt signaling pathway, e.g., for treating diseases or disorders associated with aberrant Wnt signaling. In addition, the compounds can be used as inhibitors of one or more kinases, kinase receptors, or kinase complexes (e.g., VEGF, CHK-1, CLK, HIPK, Abl, JAK and/or CDK complexes). Such compounds and compositions are also useful for controlling cellular proliferation, differentiation, and/or apoptosis.

Some embodiments of the present invention include compounds, salts, pharmaceutically acceptable salts or pro-drug thereof of formula (Ia):

In some embodiments, R¹, R², R⁴, R⁶, R⁷, R⁸ and R⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, —(C₁₋₉ alkyl)carbocyclylR¹³, —(C₁₋₉ alkyl)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl))heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R³ is selected from the group consisting of —NRS(═O)R¹⁴, —(C₁₋₉alkyl)R¹⁴, -carbocyclylR¹⁴R¹⁵, -heterocyclylR¹⁴R¹⁵, -arylR¹⁴R¹⁵ or -heteroarylR¹⁴R¹⁵.

In some embodiments, one of each R¹ and R², R² and R³, R³ and R⁴, R⁶ and R⁷, R⁷ and R⁸ or R⁸ and R⁹ are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond.

In some embodiments, each R¹⁰ is independently selected from the group consisting of H, —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl.

In some embodiments, each R¹¹ is independently selected from the group consisting of —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl.

In some embodiments, each R¹² is independently selected from the group consisting of —OR¹⁰ and R¹⁰.

In some embodiments, each R¹³ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹³, heterocyclylR¹³, arylR¹³, heteroarylR³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₄ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R¹⁴ is selected from the group consisting of —NR¹⁰C(=A)R¹⁰, —NR¹⁰S(═O)R¹⁰, —NR¹⁰SO₂R¹⁰, —NR¹⁰C(═O)N(R¹⁶)₂, —NR¹⁰C(═S)N(R¹⁰)₂, —NR¹⁰C(═NR¹²)N(R¹⁰)₂N(R¹⁶)₂, —C(═O)NR¹⁰R¹⁷, —C(═S)N(R¹⁰)₂, —C(═NR¹²)N(R¹⁰)₂, —OC(=A)R¹⁰, —C(=A)R¹⁰, —NR¹⁰C(=A)OR¹⁰ and —OC(=A)NR¹⁰R¹⁰.

In some embodiments, R^(is) is 1-4 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹³, heterocyclylR¹³, arylR¹³, heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R¹⁶ is —C₁₋₉ alkyl.

In some embodiments, each R¹⁷ is independently selected from the group consisting of -heterocyclylR¹³, —(C₁₋₉ alkyl)heterocyclylR¹³ and —(C₁₋₉ alkyl)carbocyclylR¹³.

In some embodiments, R¹⁸ and R¹⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹¹, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₄₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R¹⁸ and R¹⁹ are taken together to form a ring which is selected from the group consisting of benzene and pyridine.

In some embodiments, each A is independently selected from O, S and NR².

In some embodiments, Y¹, Y², Y³ and Y⁴ are independently selected from the group consisting of carbon and nitrogen with the proviso that at least one of Y¹, Y², Y³ and Y⁴ are nitrogen.

In some embodiments, Y¹ is nitrogen and R⁶ is absent.

In some embodiments, Y² is nitrogen and R⁷ is absent.

In some embodiments, Y³ is nitrogen and R⁸ is absent.

In some embodiments, Y⁴ is nitrogen and R⁹ is absent.

In some embodiments, each n is 0 or 1.

Some embodiments of the present invention include compounds, salts, pharmaceutically acceptable salts or pro-drug thereof of formula (Ib):

In some embodiments, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸ and R⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)C(=A)N(R alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, one of each R¹ and R², R² and R³, R³ and R⁴, R⁶ and R⁷, R⁷ and R⁸ or R⁸ and R⁹ are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl,

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond.

In some embodiments, each R¹⁰ is independently selected from the group consisting of H, —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl.

In some embodiments, each R¹¹ is independently selected from the group consisting of —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)aryl and —(C₁₋₉ alkyl)_(n)heteroaryl.

In some embodiments, each R¹² is independently selected from the group consisting of —OR¹⁰ and R¹⁰.

In some embodiments, each R¹³ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR³, heterocyclylR¹³, arylR³, heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(RO)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R¹⁸ and R¹⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰ and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰.

In some embodiments, R¹⁸ and R¹⁹ are taken together to form a ring which is selected from the group consisting of benzene and pyridine.

In some embodiments, each A is independently selected from O, S and NR¹².

In some embodiments, Y¹, Y², Y³ and Y⁴ are independently selected from the group consisting of carbon and nitrogen with the proviso that at least one of Y¹, Y², Y³ and Y⁴ are nitrogen.

In some embodiments, Y¹ is nitrogen and R⁶ is absent.

In some embodiments, Y² is nitrogen and R⁷ is absent.

In some embodiments, Y³ is nitrogen and R⁸ is absent.

In some embodiments, Y⁴ is nitrogen and R⁹ is absent.

In some embodiments, each n is 0 or 1.

Illustrative compounds of Formula (Ia) and (Ib) are shown in Table 1.

TABLE 1

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

Compound Preparation

The starting materials used in preparing the compounds of the invention are known, made by known methods, or are commercially available. It will be apparent to the skilled artisan that methods for preparing precursors and functionality related to the compounds claimed herein are generally described in the literature. The skilled artisan given the literature and this disclosure is well equipped to prepare any of the compounds.

It is recognized that the skilled artisan in the art of organic chemistry can readily carry out manipulations without further direction, that is, it is well within the scope and practice of the skilled artisan to carry out these manipulations. These include reduction of carbonyl compounds to their corresponding alcohols, oxidations, acylations, aromatic substitutions, both electrophilic and nucleophilic, etherifications, esterification and saponification and the like. These manipulations are discussed in standard texts such as March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure 6^(th) Ed., John Wiley & Sons (2007), Carey and Sundberg, Advanced Organic Chemistry 5^(th) Ed., Springer (2007), Comprehensive Organic Transformations: A Guide to Functional Group Transformations, 2^(nd) Ed., John Wiley & Sons (1999) (incorporated herein by reference in its entirety) and the like.

The skilled artisan will readily appreciate that certain reactions are best carried out when other functionality is masked or protected in the molecule, thus avoiding any undesirable side reactions and/or increasing the yield of the reaction. Often the skilled artisan utilizes protecting groups to accomplish such increased yields or to avoid the undesired reactions. These reactions are found in the literature and are also well within the scope of the skilled artisan. Examples of many of these manipulations can be found for example in T. Greene and P. Wuts Protecting Groups in Organic Synthesis, 4th Ed., John Wiley & Sons (2007), incorporated herein by reference in its entirety.

The following example schemes are provided for the guidance of the reader, and represent preferred methods for making the compounds exemplified herein. These methods are not limiting, and it will be apparent that other routes may be employed to prepare these compounds. Such methods specifically include solid phase based chemistries, including combinatorial chemistry. The skilled artisan is thoroughly equipped to prepare these compounds by those methods given the literature and this disclosure. The compound numberings used in the synthetic schemes depicted below are meant for those specific schemes only, and should not be construed as or confused with same numberings in other sections of the application.

To further illustrate this invention, the following examples are included. The examples should not, of course, be construed as specifically limiting the invention. Variations of these examples within the scope of the claims are within the purview of one skilled in the art and are considered to fall within the scope of the invention as described, and claimed herein. The reader will recognize that the skilled artisan, armed with the present disclosure, and skill in the art is able to prepare and use the invention without exhaustive examples.

Trademarks used herein are examples only and reflect illustrative materials used at the time of the invention. The skilled artisan will recognize that variations in lot, manufacturing processes, and the like, are expected. Hence the examples, and the trademarks used in them are non-limiting, and they are not intended to be limiting, but are merely an illustration of how a skilled artisan may choose to perform one or more of the embodiments of the invention.

¹H nuclear magnetic resonance spectra (NMR) were measured in the indicated solvents on a Bruker NMR spectrometer (Avance™ DRX300, 300 MHz for 1H). Peak positions are expressed in parts per million (ppm) downfield from tetramethylsilane. The peak multiplicities are denoted as follows, s, singlet; d, doublet; t, triplet; m, multiplet.

The following abbreviations have the indicated meanings:

brine=saturated aqueous sodium chloride

CDCl₃=deuterated chloroform

DCM=dichloromethane

DHP=3,4-dihydro-2H-pyran

DMF=N,N-dimethylformamide

DMSO-d₆=deuterated dimethylsulfoxide

ESIMS=electron spray mass spectrometry

EtOAc=ethyl acetate

Et₃SiH=triethylsilane

HCl=hydrochloric acid

HOAc=acetic acid

KOH=potassium hydroxide

K₃PO₄=potassium phosphate

LAH=lithium aluminum hydride

MeOH=methanol

MgSO₄=magnesium sulfate

Na₂CO₃=sodium carbonate

NaHCO₃=sodium bicarbonate

NaHSO₃=sodium bisulfite

NaOAc=sodium acetate

NMR=nuclear magnetic resonance

Pd/C=palladium on carbon

PdCl₂(dppf)₂=1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride

Pd(PPh₃)₂Cl₂=dichloro-bis(triphenylphosphine)palladium (II)

Pd(PPh₃)₄=tetrakis(triphenylphosphine)palladium(0)

PPTS=pyridinium p-toluenesulfonate

rt=room temperature

TFA=trifluoroacetic acid

THF=tetrahydrofuran

TLC=thin layer chromatography

The following example schemes are provided for the guidance of the reader, and collectively represent an example method for making the compounds provided herein. Furthermore, other methods for preparing compounds of the invention will be readily apparent to the person of ordinary skill in the art in light of the following reaction schemes and examples. Unless otherwise indicated, all variables are as defined above.

General Procedures

Compounds of Formula Ia of the present invention can be prepared as depicted in Scheme 1.

Scheme 1 describes a method for preparation of indazole derivatives (VII) by first reacting 5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde (I) with bis(pinacolato)diboron to form the borate ester (II). Suzuki coupling with various bromides (III) yields indazole derivatives (IV). Aldehyde (IV) is reacted with various 1,2-diamines (V) to produce (VI). Final deprotection of the pyrazole nitrogen yields the desired indazole derivatives (VII).

Illustrative Compound Examples

Preparation of intermediate (I) is depicted below in Scheme 2.

Reagents and conditions: a) NHOMe(Me).HCl, carbonyldiimidazole, imidazole, DMF, 65° C.; b) Bis(trifluoroacetoxy)iodobenzene, I₂, DCM r.t; c) DHP, PPTS, DCM, refluxed; d) LAH, THF, 0° C.

Step a

1H-indazole-3-carboxylic acid (VIII) (100 g, 617 mmol) in DMF was treated with carbonyldiimidazole (110 g, 678 mmol) at r.t. until the evolution of gas ceased (ca. 15 minutes). The reaction was heated to 60-65° C. for two hours and then allowed to cool to r.t. N,O-Dimethylhydroxylamine-HCl (66.2 g, 678 mmol) was added as a solid and the mixture was heated to 65° C. for 3 hours. The reaction was concentrated to a paste and taken up in DCM, and washed subsequently with water and 2N HCl. The product could be seen coming out of solution. The solid was filtered and rinsed separately with EtOAc. The EtOAc and DCM layers were separately washed with sodium bicarbonate followed by brine, dried over MgSO₄ and concentrated under reduced pressure. The resulting solids were combined, triturated with 1:1 mixture of DCM-ether, filtered, and dried to produce N-methoxy-N-methyl-1H-indazole-3-carboxamide (IX) as a white solid (100 g, 487 mmol, 79% yield). ¹H NMR (DMSO-d₆) δ ppm 3.46 (s, 3H), 3.69-3.85 (m, 3H), 7.13-7.31 (m, 1H), 7.41 (t, J=7.25 Hz, 1H), 7.56-7.65 (m, 1H), 7.93-8.08 (m, 1H); ESIMS found for C₁₀H₁₁N₃O₂ m/z 206 (M+H).

Step b

To the N-methoxy-N-methyl-1H-indazole-3-carboxamide (IX) (20 g, 97.4 mmol) in 1 L DCM was added bis(trifluoroacetoxy)iodobenzene (46 g, 107 mmol) followed by portionwise addition of iodine (14.84 g, 58.5 mmol) at r.t. After 1 hour, 600 mL of saturated NaHSO₃ was added and a solid began to precipitate which was filtered and rinsed with excess DCM. The filtrate was washed with brine, dried over MgSO₄, concentrated and the remaining solid was triturated with a minimal amount of DCM. The combined solids were dried under vacuum over KOH to produce 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (X) as a white solid (23.2 g, 70 mmol, 72% yield). ¹H NMR (DMSO-d₆) δ ppm 3.45 (s, 4H), 3.77 (s, 4H), 7.45-7.54 (m, 1H), 7.66 (dd, J=−8.81, 1.51 Hz, 1H), 8.40 (d, J=1.01 Hz, 1H); ESIMS found for C₁₀H₁₀IN₃O₂ m/z 331 (M+H).

Step c

A mixture of 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (X) (16.5 g, 50 mmol), 3,4-dihydro-2H-pyran (10.3 mL, 113 mmol) and PPTS (0.12 g, 0.6 mmol) in DCM was heated to reflux for 5 hours. The solution was poured into a saturated NaHCO₃ solution, the layers were separated, and the aqueous layer was extracted with DCM. The combined organic layers were washed with 5% aqueous citric acid and brine, dried over MgSO₄, and concentrated. The crude product was purified on a silica gel column (100% EtOAc→3:97 MeOH:DCM) to provide 5-iodo-N-methoxy-N-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carboxamide (XI) as a white viscous oil (19.1 g, 46 mmol, 92% yield). ¹H NMR (DMSO-d₆) δ ppm 1.28-1.84 (m, 6H), 3.43 (s, 3H), 3.60-4.04 (s, 5H), 5.86-6.08 (m, 1H), 7.45-7.87 (m, 2H), 8.39 (s, 1H); ESIMS found for C₁₅H₁₈IN₃O₃ m/z 416 (M+H).

Step d

Lithium aluminum hydride (160 mg, 4.21 mmol) was added in portions to a cooled (0° C.) solution of 5-iodo-N-methoxy-N-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carboxamide (XI) (1.46 g, 3.5 mmol) in THF. Stirring was continued at 0° C. until the reaction was completed, approximately 30 min. The reaction was quenched by the slow addition of EtOAc at 0° C., and the whole mixture was poured into 0.4 N NaHSO₄. The organic layer was washed with brine, dried over MgSO₄, concentrated, and purified on a silica gel column (100% EtOAc→3:97 MeOH:DCM) to give 5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde (I) as a white solid (0.90 g, 3.15 mmol, 72% yield). ¹H NMR (DMSO-d₆) δ ppm 1.50-1.71 (m, 2H), 1.71-1.87 (m, 1H), 1.97-2.15 (m, 2H), 2.31-2.42 (m, 1H), 3.66-3.99 (m, 2H), 5.96-6.17 (m, 1H), 7.78 (d, J=6 Hz, 1H), 7.84 (d, J=6 Hz, 1H), 8.50 (s, 1H), 10.13 (s, 1H); ESIMS found for C₁₃H₁₃IN₂O₂ m/z 357 (M+H).

Preparation of intermediate (XV) is depicted below in Scheme 3.

Reagents and conditions: a) HOAc, NaOAc, Br₂, 100° C., 28 h, b) 1,4-Dioxane, pyridyl-3-boronic acid, Na₂CO₃, H₂O, Pd(PPh₃)₂Cl₂, reflux., 15 h, c) MeOH, Pd/C, H₂, rt, 15 h

Step a

A mixture of 3-nitropyridin-4-amine (XII) (10 g, 71.94 mmol) and acetic acid (120 ml) was added to a sealed tube followed by addition of NaOAc (29.50 g, 93.52 mmol) and dropwise addition of bromine (4.7 ml 359.7 mmol) under stirring. The sealed tube was heated at 100° C. for 28 h until TLC showed consumption of starting material. The reaction mixture was concentrated to obtain a solid which was dissolved in water, basified with NaHCO₃ and extracted with ethyl acetate. The combined organic extracts were dried and concentrated to produce 3-bromo-5-nitropyridin-4-amine (XIII) as a yellow solid (12 g, 55 mmol, 77% yield). ¹H NMR (DMSO-d₆) δ ppm 9.19 (s, 1H), 8.58 (s, 1H); ESIMS found for C₅H₄BrN₃O₂ m/z 217, 219 (M+, M+2).

Step b

A solution of 3-bromo-5-nitropyridin-4-amine (XIII) (6 g, 26 mmol), pyridin-3-ylboronic acid (3.54 g, 29 mmol), 1 N Na₂CO₃ solution (78 ml) and 1,4-dioxane (150 mL) was degassed with argon thrice. Pd(PPh₃)₂Cl₂ (927 mg, 5 mmol %) was added to the reaction and the solution was refluxed for 15 h until TLC showed the reaction was complete. The reaction was passed through a pad of Celite and then concentrated under reduced pressure. The reaction mixture was concentrated and the residue was taken up in ethyl acetate. The organic extract was washed with water, dried and concentrated under vacuum. The crude product was purified on a silica gel column (100% EtOAc→2:98 MeOH:DCM) to give 5-nitro-3,3′-bipyridin-4-amine (XIV) as a yellow solid (5 g, 23.1 mmol, 87% yield). ¹H NMR (CDCl₃, 400 MHz,) δ ppm 9.31 (s, 1H), 8.80-8.79 (m, 1H), 8.70 (s, 1H), 8.23 (s, 1H), 7.80-7.73 (m, 1H), 7.52-7.48 (m, 1H). ESIMS found C₁₀H₈N₄O₂ m/z 216.95 (M+H).

Step c

To a solution of 5-nitro-3,3′-bipyridin-4-amine (XIV) (5 g, 23 mmol) in MeOH (20 mL) was added 10% Pd/C. The solution was purged with hydrogen and stirred at r.t. under hydrogen for 15 h. The suspension was filtered through Celite and the concentrated under vacuum to produce 3,3′-bipyridine-4,5-diamine (XV) as off white solid (3.3 g, 17.7 mmol, 76% yield). ¹H NMR (DMSO-d6, 400 MHz,): δ 8.63-8.53 (m, 1H), 7.90-7.83 (m, 1H), 7.75 (s, 1H), 7.58 (s, 1H), 7.48-7.43 (m, 2H), 6.13 (bs, 2H), 5.31 (bs, 2H). ESIMS found C₁₀H₁₀N₄ m/z 187.10 (M+H).

Preparation of intermediate (XVII) is depicted below in Scheme 4.

Step 1-2

To a solution of 5-bromonicotinic acid (XVI) (1.01 g, 5 mmol) in dry DCM (10 mL) under nitrogen was added oxalyl chloride (0.654 mL, 7.5 mmol) followed by dry DMF (0.1 mL). The solution was stirred at r.t. for 30 min. The solvent was evaporated under vacuum before adding dry pyridine (10 mL) followed by cyclopropylmethanamine (0.39 mL, 4.5 mmol). The solution was stirred at r.t. under nitrogen for 2 h. The solution was poured into ice water, basified with sat. aq. NaHCO₃ and extracted with DCM. The combined organic phases were dried over MgSO₄, concentrated and dried under vacuum to yield 5-bromo-N-(cyclopropylmethyl) nicotinamide (XVII) as an off-white solid (0.82 g, 3.2 mmol, 71% yield). ¹H NMR (DMSO-d₆) δ ppm −0.07-0.07 (m, 2H), 0.15-0.29 (m, 2H), 0.68-0.88 (m, 1H), 2.93 (t, J=6.22 Hz, 2H), 8.20 (t, J=1.88 Hz, 1H), 8.62 (d, J=1.70 Hz, 2H), 8.75 (s, 1H); ESIMS found C₁₀H₁₁BrN₂O m/z 254, 256 (M+, M+2).

Preparation of intermediate (XX) is depicted below in Scheme 5.

Step 1

3-Amino-5-bromo pyridine (XVIII) (1 eq) was dissolved in DCM and cooled to 0° C. before adding pyridine (2.2 eq) and isobutyryl chloride (XIX) (1.1 eq). The reaction mixture was stirred at r.t. for 15 h until TLC showed the reaction was complete. The reaction mixture was diluted with DCM and washed with water. The organic extract was dried, concentrated and purified by column chromatography using silica gel (100-200 mesh) to afford N-(5-bromopyridin-3-yl)isobutyramide (XX) as a off white solid, (71% yield). ¹H NMR (CDCl₃) δ ppm 8.55-8.35 (m, 3H), 7.32 (s, 1H), 2.59-2.48 (m, 1H), 1.28-1.27 (d, 6H); ESIMS found C₉H₁₁BrN₂O m/z 243.05 (M+H).

The following intermediates were prepared in accordance with the procedure described in the above Scheme 5.

N-(5-bromopyridin-3-yl)pivalamide (XXI): Off white solid, (67%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.48-8.39 (m, 3H), 7.48 (bs, 1H), 1.32 (s, 9H); ESIMS found C₁₀H₁₃BrN₂O m/z 256.80 (M+H).

N-(5-bromopyridin-3-yl)-3-methylbutanamide (XXII): white solid, (67% yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.55-8.42 (m, 3H), 7.62 (s, 1H), 2.31-2.18 (m, 3H), 1.02-1.01 (d, J=6 Hz, 6H); ESIMS found C₁₀H₁₃BrN₂O m/z 258.80 (M+H).

N-(5-bromopyridin-3-yl)-3,3-dimethylbutanamide (XXIII): Light yellow solid, (64%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.48 (s, 1H), 8.40 (s, 1H), 7.62 (s, 1H), 7.20 (bs, 1H), 2.26 (s, 3H), 1.10 (s, 9H); ESIMS found C₁₁H₁₅BrN₂O m/z 272.80 (M+H).

N-(5-bromopyridin-3-yl)butyramide (XXIV): Yellow solid, (86%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.48-8.39 (m, 3H), 7.38 (bs, 1H), 2.40-2.36 (t, J=7.2 Hz, 2H), 1.81-1.72 (m, 2H), 1.03-0.98 (t, J=7.2 Hz, 3H); ESIMS found C₉H₁₁BrN₂O m/z 242.90 (M+H).

N-(5-bromopyridin-3-yl)pentanamide (XXV): Off white solid, (75%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.47-8.39 (m, 3H), 7.33 (bs, 1H), 2.41-2.38 (t, 2H, J=7.6 Hz, 2H), 1.75-1.68 (m, 2H), 1.45-1.36 (m, 2H), 0.97-0.93 (t, J=7.2 Hz, 3H); ESIMS found C₁₀H₁₃BrN₂O m/z 256.90 (M+H).

N-(5-bromopyridin-3-yl)cyclopropanecarboxamide (XXVI): Off white solid, (83% yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.46-8.39 (m, 3H), 7.54 (bs, 1H), 1.56-1.50 (m, 1H), 1.13-1.07 (m, 2H), 0.96-0.90 (m, 2H); ESIMS found C₉H₉BrN₂O m/z 240.85 (M+H).

N-(5-bromopyridin-3-yl)cyclobutanecarboxamide (XXVII): Off white solid, (54% yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.97-8.39 (m, 3H), 7.21 (bs, 1H), 3.20-3.16 (m, 1H), 2.42-2.24 (m, 4H), 2.05-1.94 (m, 2H); ESIMS found C₁₀H₁₁BrN₂O m/z 256.90 (M+H).

N-(5-bromopyridin-3-yl)cyclohexanecarboxamide (XXVIII): light yellow solid, (89% yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.49-8.38 (m, 3H), 7.61 (bs, 1H), 2.30-2.23 (dd, 1H, J=3.2 Hz, J=11.6 Hz, 1H), 1.96-1.49 (m, 4H), 1.34-1.19 (m, 3H); ESIMS found C₁₂H₁₅BrN₂O m/z 284.75 (M+H).

N-(5-bromopyridin-3-yl)benzamide (XXIX): Off white solid, (85%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.58-8.57 (m, 2H), 8.44-4.43 (d, J=1.6 Hz, 1H), 8.03 (bs, 1H), 7.88-7.86 (d, J=7.2 Hz, 2H), 7.61-7.49 (m, 3H); ESIMS found C₁₂H₁₉BrN₂O m/z 278.75 (M+H).

N-(5-bromopyridin-3-yl)-2-phenylacetamide (XXX): Off white solid, (59%, yield), ¹H NMR (CDCl₃, 400 MHz) δ ppm 8.37-8.31 (m, 3H), 7.41-7.30 (m, 6H), 3.75 (s, 2H); ESIMS found C₁₃H₁₁BrN₂O m/z 292.72 (M+H).

Example 1

Preparation of compound (3) is depicted below in Scheme 6.

Reagents and conditions: a) KOAc, PdCl₂(dppf)₂, DMF, 80° C., 2 h; b) K₂PO₄, Pd(PPh₃)₄, DMF, H₂O, 90° C., 3 h; c) DMF, sulfur, 140° C., ON; d) Et₃SiH, DCM, TFA, r.t., 2 h.

Step a-b

A solution of 5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde (I) (1.068 g, 3.0 mmol), bis(pinacolato)diboron (0.914 g, 3.6 mmol), KOAc (0.883 g, 9.0 mmol) and dry DMF (20 mL) was purged with nitrogen. PdCl₂(dppf)₂ was added to the reaction and purged again with nitrogen. The solution was heated at 80° C. for 2 h. Once TLC showed the disappearance of (I), the solution was cooled to r.t. To this solution was added K₃PO₄ (0.955 g, 4.5 mmol), 5-bromo-N-(cyclopropylmethyl) nicotinamide (XVII) (0.765 g, 3.0 mmol), Pd(PPh₃)₄ (104 mg, 0.09 mmol) and water (2 mL). The solution was purged with nitrogen and heated at 90° C. for 3 h. The reaction was passed through a pad of Celite and then concentrated under reduced pressure. The residue was dissolved in DCM and washed with water and brine, dried over MgSO₄ and then evaporated under vacuum. The crude product was purified on a silica gel column (100% EtOAc→2:98 MeOH:DCM) to give N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide (XXXI) as a yellow solid (1.09 g, 2.7 mmol, 90% yield). ¹H NMR (DMSO-d₆) δ ppm 0.20-0.31 (m, 2H), 0.35-0.57 (m, 2H), 1.65 (m, 2H), 1.74-1.87 (m, 1H), 2.10 (d, J=12.06 Hz, 2H), 2.35-2.44 (m, 1H), 3.10-3.27 (m, 3H), 3.78-3.99 (m, 2H), 6.14 (d, J=7.35 Hz, 1H), 7.90-8.14 (m, 2H), 8.50 (d, J=12.5, 2H), 9.05 (dd, J=14.60, 1.98 Hz, 2H), 10.25 (s, 1H); ESIMS found C₂H₂₄N₄O₃ m/z 405 (M+H).

Step c

A solution of N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide (XXXI) (0.404 g, 1.0 mmol), 3,3′-bipyridine-4,5-diamine (XV) (186 mg, 1.0 mmol) and sulfur (35 mg, 1.1 mmol) in dry DMF (10 mL) was heated at 140° C. overnight. The reaction was cooled and evaporated under vacuum. The residue was suspended in water, sonicated and filtered. The solid was washed with cold water and dried under vacuum. The crude product was dissolved in DCM and cooled to 4° C. overnight to get N-(cyclopropylmethyl)-5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl) nicotinamide (XXII) as a brown solid (130 mg, 0.23 mmol, 23% yield). ¹H NMR (DMSO-d₆) δ ppm 0.19-0.37 (m, 2H), 0.36-0.58 (m, 2H), 0.97-1.115 (m, 1H), 1.67 (br, 2H), 2.14 (d, J=9.98 Hz, 2H), 2.40-2.46 (m, 1H), 3.20-3.33 (m, 3H), 3.75-4.14 (m, 2H), 6.13 (d, J=8.29 Hz, 1H), 7.60 (dd, J=7.82, 4.80 Hz, 1H), 7.92-8.12 (m, 3H), 8.20 (d, J=8.67 Hz, 1H), 8.55-8.67 (m, 2H), 8.94 (br s, 3H), 9.06 (d, J=1.88 Hz, 1H), 9.19 (d, J=1.87 Hz, 1H); ESIMS found C₃₃H₃₀N₈O₂ m/z 571 (M+H).

Step d

A solution of N-(cyclopropylmethyl)-5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide (XXXII) (125 mg, 0.22 mmol) and Et₃SiH (87 μL, 0.55 mmol) in DCM (5 mL) was slowly added TFA (2.5 mL). The reaction was stirred at r.t. for 3 h. The reaction was evaporated under vacuum and the residue was treated with water, basified with aq. ammonia. The solids were filtered, washed with cold water and dried. The crude product was heated in MeOH and filtered hot to remove impurities. The hot MeOH solution was allowed to slowly cool to r.t. to produce N-(cyclopropylmethyl)-5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)nicotinamide (3) as a off-white solid (48 mg, 0.10 mmol, 44% yield). ¹H NMR (DMSO-d₆) δ ppm 0.28 (d, J=4.28 Hz, 2H), 0.42-0.58 (m, 2H), 1.09 (br s, 1H), 3.25 (t, J=6.06 Hz, 2H), 7.50-7.70 (m, 1H), 7.79-8.11 (m, 2H), 8.48-8.68 (m, 1H), 8.69-8.82 (m, 1H), 8.81-8.97 (m, 3H), 9.00-9.18 (m, 2H), 9.46 (br s, 1H); ESIMS found C₂₈H₂₂N₈ m/z 487 (M+H).

The following compounds was prepared in accordance with the procedure described in the above Example 1.

5-(3-(3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)-N-(piperidin-4-yl)nicotinamide 1

¹H NMR (DMSO-d₆) δ ppm 1.55-1.75 (m, 2H), 1.90-2.05 (m, 2H), 2.78-2.90 (t, 2H), 3.15-3.25 (d, 2H), 3.95-4.12 (m, 1H), 7.65 (br s, 1H), 7.87 (dd, 2H), 8.31 (d, 1H), 8.53 (s, 1H), 8.79 (s, 1H), 8.98 (s, 2H), 9.13 (s, 1H); ESIMS found for C₂₄H₂₂N₈O m/z 439 (M+H).

5-(3-(3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)-N-(cyclohexyl methyl)nicotinamide 2

¹H NMR (DMSO-d₆) δ ppm 0.98-1.15 (m, 2H), 1.2-1.39 (m, 3H), 1.64-1.89 (m, 6H), 3.21-3.35 (m, 2H), 7.73 (d, 1H), 7.82 (d, 1H), 7.88 (d, 1H), 8.34 (s, 1H), 8.62 (s, 1H), 8.86 (s, 1H), 8.96 (s, 1H), 8.99 (s, 1H), 9.12 (s, 1H); ESIMS found for C₂₆H₂₅N₇O m/z 452 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)propionamide 4

¹H NMR (DMSO-d₆) δ ppm 1.15 (t, J=7.16 Hz, 3H), 2.40 (q, 2H), 7.60 (br s, 1H), 7.85 (br s, 3H), 8.39-8.54 (m, 1H), 8.66 (br s, 2H), 8.77 (s, 1H), 8.82 (s, 1H), 8.97 (br s, 1H); ESIMS found for C₂₆H₂₀N₈O m/z 461 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)isobutyramide 11

Dark brown solid (40% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.01 (br s, 1H), 13.79 (br s, 1H), 10.19 (s, 1H), 9.42 (s, 1H), 8.87-8.47 (m, 8H), 7.83-7.78 (m, 2H), 7.57-7.54 (m, 1H), 2.69-2.62 (m, 2H), 1.14-1.13 (d, J=6.8 Hz, 6H). ESIMS found C₂₇H₂₂N₈)O m/z 475.10 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)cyclopropanecarboxamide 12

Dark brown solid (23% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.03 (s, 1H), 13.80 (s, 1H), 10.59 (s, 1H), 9.45 (s, 1H), 8.92-8.65 (m 7H), 8.47 (s, 1H), 7.83 (s, 2H), 7.57 (s, 1H), 1.88-1.86 (m, 1H), 0.88-0.87 (m, 4H). ESIMS found C₂₇H₂₀N₈O m/z 473.15 (M+H).

3-methyl-N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)butanamide 15

Dark brown solid (14% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.03 (s, 1H), 13.78 (br s, 1H), 10.24 (s, 1H), 9.46 (s, 1H), 8.89-8.76 (m, 4H), 8.75-8.39 (m, 4H), 7.86-7.82 (m, 2H), 7.59-7.58 (m, 1H), 2.30-2.28 (d, J=6.8 Hz, 2H), 2.18-2.12 (m, 1H), 0.99-097 (d, J=6.4 Hz, 6H). ESIMS found C₂₈H₂₄N₈O m/z 489.20 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)benzamide 16

Dark brown solid (30% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.04 (s, 1H), 13.80 (s, 1H), 10.63 (s, 1H), 9.45 (s, 1H), 9.00-8.74 (m, 6H), 8.63 (s, 1H), 8.36 (s, 1H), 8.07-8.05 (m, 2H), 7.88-7.86 (m, 2H), 7.67-7.52 (m, 4H). ESIMS found C₃₀H₂₀N₈O m/z 509.05 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)pivalamide 17

Dark brown solid (43% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.03 (s, 1H), 13.79 (br s, 1H), 9.57 (s, 1H), 9.46 (s, 1H), 8.92-8.81 (m, 4H), 8.75-8.49 (m, 4H), 7.84 (s, 2H), 7.59-7.56 (m, 1H), 1.29 (s, 9H). ESIMS found C₂₈H₂₄N₈O m/z 489.15 (M+H).

3,3-dimethyl-N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)butanamide 18

Dark brown solid (32% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.03 (s, 1H), 13.77 (s, 1H), 10.18 (s, 1H), 9.46 (s, 1H), 8.89-8.75 (m, 4H), 8.65-8.40 (m, 2H), 7.86-7.79 (m, 2H), 7.59-7.56 (m, 2H), 2.29 (s, 2H), 1.06 (s, 9H). ESIMS found C₂₉H₂₆N₈O m/z 503.15 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)cyclohexanecarboxamide 19

Off white solid (17% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.04 (s, 1H), 13.78 (s, 1H), 10.20 (s, 1H), 9.45 (s, 1H), 8.89-8.51 (m, 7H), 7.83 (s, 2H), 7.59 (s, 2H), 1.90-1.66 (m, 5H), 1.47-1.22 (m, 6H). ESIMS found C₃₀H₂₆N8O m/z 515.15 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)butyramide 20

Dark brown solid (34% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.07 (s, 1H), 10.26 (s, 1H), 9.40 (s, 1H), 8.96 (s, 1H), 8.80-8.65 (m, 6H), 8.48 (s, 2H), 7.87-7.81 (m, 2H), 7.62-7.59 (m, 1H), 2.41-2.38 (t, J=7.2 Hz, 2H), 1.70-1.64 (m, 2H), 0.98-0.94 (t, J=7.2 Hz, 3H). ESIMS found C₂₇H₂₂N₈O m/z 475.10 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)cyclobutanecarboxamide 21

Off white solid (21% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 13.09 (s, 1H), 13.06 (s, 1H), 10.11 (s, 1H), 9.43 (bs, 1H), 8.92-8.78 (m 6H), 8.49 (s, 2H), 7.82 (s, 2H), 7.58-7.56 (m, 1H), 2.31-2.27 (m, 4H), 2.19-2.17 (m, 2H), 2.02-1.95 (m, 1H). ESIMS found C₂₈H₂₂N₈O m/z 487.10 (M+H).

2-phenyl-N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)acetamide 22

Off white solid (40% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 13.99 (s, 1H), 13.00 (s, 1H), 10.58 (s, 1H), 9.41 (s, 1H), 8.90-8.49 (m, 8H), 7.85-7.83 (m, 2H), 7.52-7.27 (m, 6H), 3.76 (s, 2H). ESIMS found C₃₁H₂₂N80 m/z 523.15 (M+H).

N-(5-(3-(7-(pyridin-3-yl)-3H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-5-yl)pyridin-3-yl)pentanamide 23

Dark brown solid (28% yield). ¹H NMR (DMSO-d₆, 400 MHz,) δ ppm 14.05 (s, 1H), 13.01 (s, 1H), 10.26 (s, 1H), 9.39 (s, 1H), 8.95-8.65 (m 7H), 8.47 (s, 1H), 7.86-7.80 (m, 2H), 7.61-7.58 (m, 1H), 2.43-2.40 (t, J=7.2 Hz, 2H), 1.65-1.59 (m, 2H), 1.40-1.34 (m, 2H), 0.94-0.90 (t, J=7.2 Hz, 3H). ESIMS found C₂₈H₂₄N₈O m/z 489.15 (M+H).

Administration and Pharmaceutical Compositions

Some embodiments include pharmaceutical compositions comprising: (a) a safe and therapeutically effective amount of the indazole, or its corresponding enantiomer, diastereoisomer or tautomer, or pharmaceutically acceptable salt; and (b) a pharmaceutically acceptable carrier.

Administration of the compounds disclosed herein or the pharmaceutically acceptable salts thereof can be via any of the accepted modes of administration for agents that serve similar utilities including, but not limited to, orally, subcutaneously, intravenously, intranasally, topically, transdermally, intraperitoneally, intramuscularly, intrapulmonarilly, vaginally, rectally, or intraocularly. Oral and parenteral administrations are customary in treating the indications.

Compounds of the invention intended for pharmaceutical use may be administered as crystalline or amorphous products. Pharmaceutically acceptable compositions include solid, semi-solid, liquid and aerosol dosage forms, such as, e.g., tablets, capsules, powders, liquids, suspensions, suppositories, aerosols or the like. They may be obtained, for example, as films by methods such as precipitation, crystallization, freeze drying, spray drying, or evaporative drying. Microwave or radio frequency drying may be used for this purpose. The compounds can also be administered in sustained or controlled release dosage forms, including depot injections, osmotic pumps, pills, transdermal (including electrotransport) patches, and the like, for prolonged and/or timed, pulsed administration at a predetermined rate. Preferably, the compositions are provided in unit dosage forms suitable for single administration of a precise dose.

The compounds can be administered either alone or more typically in combination with a conventional pharmaceutical carrier, excipient or the like. The term “excipient” is used herein to describe any ingredient other than the compound(s) of the invention. Pharmaceutically acceptable excipients include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-α-tocopherol polyethylene glycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium-chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethyl cellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, and wool fat. Cyclodextrins such as α-, β, and γ-cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3-hydroxypropyl-b-cyclodextrins, or other solubilized derivatives can also be advantageously used to enhance delivery of compounds of the formulae described herein. Dosage forms or compositions containing a compound as described herein in the range of 0.005% to 100% with the balance made up from non-toxic carrier may be prepared. The contemplated compositions may contain 0.001%-100% active ingredient, in one embodiment 0.1-95%, in another embodiment 75-85%. Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington: The Science and Practice of Pharmacy, 21 st Edition (Lippincott Williams & Wilkins. 2005).

In one preferred embodiment, the compositions will take the form of a unit dosage form such as a pill or tablet and thus the composition may contain, along with the active ingredient, a diluent such as lactose, sucrose, dicalcium phosphate, or the like; a lubricant such as magnesium stearate or the like; and a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives or the like. In another solid dosage form, a powder, marume, solution or suspension (e.g., in propylene carbonate, vegetable oils or triglycerides) is encapsulated in a gelatin capsule. Unit dosage forms in which the two active ingredients are physically separated are also contemplated; e.g., capsules with granules of each drug; two-layer tablets; two-compartment gel caps, etc.

Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing, etc. an active compound as defined above and optional pharmaceutical adjuvants in a carrier (e.g., water, saline, aqueous dextrose, glycerol, glycols, ethanol or the like) to form a solution or suspension. If desired, the pharmaceutical composition can also contain minor amounts of nontoxic auxiliary substances such as wetting agents, emulsifying agents, solubilizing agents, pH buffering agents and the like (e.g., sodium acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine acetate, triethanolamine oleate, and the like). Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, as emulsions, or in solid forms suitable for dissolution or suspension in liquid prior to injection. The percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject. However, percentages of active ingredient of 0.01% to 10% in solution are employable, and will be higher if the composition is a solid, which will be subsequently diluted to the above percentages. In some embodiments, the composition will comprise 0.2-2% of the active agent in solution.

It is to be noted that concentrations and dosage values may also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular patient, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed compositions.

Solid compositions can be provided in various different types of dosage forms, depending on the physicochemical properties of the drug, the desired dissolution rate, cost considerations, and other criteria. In one of the embodiments, the solid composition is a single unit. This implies that one unit dose of the drug is comprised in a single, physically shaped solid form or article. In other words, the solid composition is coherent, which is in contrast to a multiple unit dosage form, in which the units are incoherent.

Examples of single units which may be used as dosage forms for the solid composition include tablets, such as compressed tablets, film-like units, foil-like units, wafers, lyophilized matrix units, and the like. In a preferred embodiment, the solid composition is a highly porous lyophilized form. Such lyophilizates, sometimes also called wafers or lyophilized tablets, are particularly useful for their rapid disintegration, which also enables the rapid dissolution of the active compound.

On the other hand, for some applications the solid composition may also be formed as a multiple unit dosage form as defined above. Examples of multiple units are powders, granules, microparticles, pellets, beads, lyophilized powders, and the like. In one embodiment, the solid composition is a lyophilized powder. Such a dispersed lyophilized system comprises a multitude of powder particles, and due to the lyophilization process used in the formation of the powder, each particle has an irregular, porous microstructure through which the powder is capable of absorbing water very rapidly, resulting in quick dissolution.

Another type of multiparticulate system which is also capable of achieving rapid drug dissolution is that of powders, granules, or pellets from water-soluble excipients which are coated with the drug, so that the drug is located at the outer surface of the individual particles. In this type of system, the water-soluble low molecular weight excipient is useful for preparing the cores of such coated particles, which can be subsequently coated with a coating composition comprising the drug and, preferably, one or more additional excipients, such as a binder, a pore former, a saccharide, a sugar alcohol, a film-forming polymer, a plasticizer, or other excipients used in pharmaceutical coating compositions.

Also provided herein are kits. Typically, a kit includes one or more compounds or compositions as described herein. In certain embodiments, a kit can include one or more delivery systems, e.g., for delivering or administering a compound as provided above, and directions for use of the kit (e.g., instructions for treating a patient). In another embodiment, the kit can include a compound or composition as described herein and a label that indicates that the contents are to be administered to a patient with cancer. In another embodiment, the kit can include a compound or composition as described herein and a label that indicates that the contents are to be administered to a patient with one or more of hepatocellular carcinoma, colon cancer, leukemia, lymphoma, sarcoma, ovarian cancer, diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, psoriasis, mycotic and viral infections, osteochondrodysplasia, Alzheimer's disease, osteoarthritis, polyposis coli, osteoporosis-pseudoglioma syndrome, familial exudative vitreoretinopathy, retinal angiogenesis, early coronary disease, tetra-amelia syndrome, Müllerian-duct regression and virilization, SERKAL syndrome, diabetes mellitus type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity, split-hand/foot malformation, caudal duplication syndrome, tooth agenesis, Wilms tumor, skeletal dysplasia, focal dermal hypoplasia, autosomal recessive anonychia, neural tube defects, alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF syndrome, Angelman syndrome, Prader-Willi syndrome, Beckwith-Wiedemann Syndrome and Rett syndrome.

The actual dose of the active compounds of the present invention depends on the specific compound, and on the condition to be treated; the selection of the appropriate dose is well within the knowledge of the skilled artisan.

Methods of Treatment

The compounds and compositions provided herein can be used as inhibitors of one or more members of the Wnt pathway, including one or more Wnt proteins, and thus can be used to treat a variety of disorders and diseases in which aberrant Wnt signaling is implicated, such as cancer and other diseases associated with abnormal angiogenesis, cellular proliferation, and cell cycling. Accordingly, the compounds and compositions provided herein can be used to treat cancer, to reduce or inhibit angiogenesis, to reduce or inhibit cellular proliferation and correct an genetic disorder due to mutations in Wnt signaling components. Non-limiting examples of diseases which can be treated with the compounds and compositions provided herein include a variety of cancers, diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, psoriasis, mycotic and viral infections, osteochondrodysplasia, Alzheimer's disease, osteoarthritis, polyposis coli, osteoporosis-pseudoglioma syndrome, familial exudative vitreoretinopathy, retinal angiogenesis, early coronary disease, tetra-amelia syndrome, Müllerian-duct regression and virilization, SERKAL syndrome, diabetes mellitus type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity, split-hand/foot malformation, caudal duplication syndrome, tooth agenesis, Wilms tumor, skeletal dysplasia, focal dermal hypoplasia, autosomal recessive anonychia, neural tube defects, alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF syndrome, Angelman syndrome, Prader-Willi syndrome, Beckwith-Wiedemann Syndrome and Rett syndrome.

With respect to cancer, the Wnt pathway is known to be constitutively activated in a variety of cancers including, for example, colon cancer, hepatocellular carcinoma, lung cancer, ovarian cancer, prostate cancer, pancreatic cancer and leukemias such as CML, CLL and T-ALL. The constitutive activation is due to constitutively active β-catenin, perhaps due to its stabilization by interacting factors or inhibition of the degradation pathway. Accordingly, the compounds and compositions described herein may be used to treat these cancers in which the Wnt pathway is constitutively activated. In certain embodiments, the cancer is chosen from hepatocellular carcinoma, colon cancer, leukemia, lymphoma, sarcoma and ovarian cancer.

Other cancers can also be treated with the compounds and compositions described herein.

More particularly, cancers that may be treated by the compound, compositions and methods described herein include, but are not limited to, the following:

1) Breast cancers, including, for example ER⁺ breast cancer, ER⁻ breast cancer, her2⁻ breast cancer, her2⁺ breast cancer, stromal tumors such as fibroadenomas, phyllodes tumors, and sarcomas, and epithelial tumors such as large duct papillomas; carcinomas of the breast including in situ (noninvasive) carcinoma that includes ductal carcinoma in situ (including Paget's disease) and lobular carcinoma in situ, and invasive (infiltrating) carcinoma including, but not limited to, invasive ductal carcinoma, invasive lobular carcinoma, medullary carcinoma, colloid (mucinous) carcinoma, tubular carcinoma, and invasive papillary carcinoma; and miscellaneous malignant neoplasms. Further examples of breast cancers can include luminal A, luminal B, basal A, basal B, and triple negative breast cancer, which is estrogen receptor negative (ER⁻), progesterone receptor negative, and her2 negative (her2⁻). In some embodiments, the breast cancer may have a high risk Oncotype score.

2) Cardiac cancers, including, for example sarcoma, e.g., angiosarcoma, fibrosarcoma, rhabdomyosarcoma, and liposarcoma; myxoma; rhabdomyoma; fibroma; lipoma and teratoma.

3) Lung cancers, including, for example, bronchogenic carcinoma, e.g., squamous cell, undifferentiated small cell, undifferentiated large cell, and adenocarcinoma; alveolar and bronchiolar carcinoma; bronchial adenoma; sarcoma; lymphoma; chondromatous hamartoma; and mesothelioma.

4) Gastrointestinal cancer, including, for example, cancers of the esophagus, e.g., squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, and lymphoma; cancers of the stomach, e.g., carcinoma, lymphoma, and leiomyosarcoma; cancers of the pancreas, e.g., ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma, carcinoid tumors, and vipoma; cancers of the small bowel, e.g., adenocarcinoma, lymphoma, carcinoid tumors, Kaposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, and fibroma; cancers of the large bowel, e.g., adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, and leiomyoma.

) Genitourinary tract cancers, including, for example, cancers of the kidney, e.g., adenocarcinoma, Wilm's tumor (nephroblastoma), lymphoma, and leukemia; cancers of the bladder and urethra, e.g., squamous cell carcinoma, transitional cell carcinoma, and adenocarcinoma; cancers of the prostate, e.g., adenocarcinoma, and sarcoma; cancer of the testis, e.g., seminoma, teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma, sarcoma, interstitial cell carcinoma, fibroma, fibroadenoma, adenomatoid tumors, and lipoma.

6) Liver cancers, including, for example, hepatoma, e.g., hepatocellular carcinoma; cholangiocarcinoma; hepatoblastoma; angiosarcoma; hepatocellular adenoma; and hemangioma.

7) Bone cancers, including, for example, osteogenic sarcoma (osteosarcoma), fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma, malignant giant cell tumor chordoma, osteochrondroma (osteocartilaginous exostoses), benign chondroma, chondroblastoma, chondromyxofibroma, osteoid osteoma and giant cell tumors.

8) Nervous system cancers, including, for example, cancers of the skull, e.g., osteoma, hemangioma, granuloma, xanthoma, and osteitis deformans; cancers of the meninges, e.g., meningioma, meningiosarcoma, and gliomatosis; cancers of the brain, e.g., astrocytoma, medulloblastoma, glioma, ependymoma, germinoma (pinealoma), glioblastoma multiform, oligodendroglioma, schwannoma, retinoblastoma, and congenital tumors; and cancers of the spinal cord, e.g., neurofibroma, meningioma, glioma, and sarcoma.

9) Gynecological cancers, including, for example, cancers of the uterus, e.g., endometrial carcinoma; cancers of the cervix, e.g., cervical carcinoma, and pre tumor cervical dysplasia; cancers of the ovaries, e.g., ovarian carcinoma, including serous cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified carcinoma, granulosa theca cell tumors, Sertoli Leydig cell tumors, dysgerminoma, and malignant teratoma; cancers of the vulva, e.g., squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, and melanoma; cancers of the vagina, e.g., clear cell carcinoma, squamous cell carcinoma, botryoid sarcoma, and embryonal rhabdomyosarcoma; and cancers of the fallopian tubes, e.g., carcinoma.

10) Hematologic cancers, including, for example, cancers of the blood, e.g., acute myeloid leukemia, chronic myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferative diseases, multiple myeloma, and myelodysplastic syndrome, Hodgkin's lymphoma, non Hodgkin's lymphoma (malignant lymphoma) and Waldenström's macroglobulinemia.

11) Skin cancers and skin disorders, including, for example, malignant melanoma, basal cell carcinoma, squamous cell carcinoma, Kaposi's sarcoma, moles dysplastic nevi, lipoma, angioma, dermatofibroma, keloids, and psoriasis.

12) Adrenal gland cancers, including, for example, neuroblastoma.

Cancers may be solid tumors that may or may not be metastatic. Cancers may also occur, as in leukemia, as a diffuse tissue. Thus, the term “tumor cell,” as provided herein, includes a cell afflicted by any one of the above identified disorders.

A method of treating cancer using a compound or composition as described herein may be combined with existing methods of treating cancers, for example by chemotherapy, irradiation, or surgery (e.g., oophorectomy). In some embodiments, a compound or composition can be administered before, during, or after another anticancer agent or treatment.

The compounds and compositions described herein can be used as anti-angiogenesis agents and as agents for modulating and/or inhibiting the activity of protein kinases, thus providing treatments for cancer and other diseases associated with cellular proliferation mediated by protein kinases. For example, the compounds described herein can inhibit the activity of one or more kinases, such as CDKs, VEGF, CLK, HIPK, Abl, JAK and CHK-1, or cyclin complexes thereof. Accordingly, provided herein is a method of treating cancer or preventing or reducing angiogenesis through kinase inhibition, such as through inhibition of VEGF, CHK-1, CLK, HIPK, Abl, JAK, CDK4 or CDK4/D-type cyclin complexes and/or CDK2 or CDK2/E-type cyclin complexes.

In addition, and including treatment of cancer, the compounds and compositions described herein can function as cell-cycle control agents for treating proliferative disorders in a patient. Disorders associated with excessive proliferation include, for example, cancers, psoriasis, immunological disorders involving undesired proliferation of leukocytes, and restenosis and other smooth muscle disorders. Furthermore, such compounds may be used to prevent de-differentiation of post-mitotic tissue and/or cells.

Diseases or disorders associated with uncontrolled or abnormal cellular proliferation include, but are not limited to, the following:

-   -   a variety of cancers, including, but not limited to, carcinoma,         hematopoietic tumors of lymphoid lineage, hematopoietic tumors         of myeloid lineage, tumors of mesenchymal origin, tumors of the         central and peripheral nervous system and other tumors including         melanoma, seminoma and Kaposi's sarcoma.     -   a disease process which features abnormal cellular         proliferation, e.g., benign prostatic hyperplasia, familial         adenomatosis polyposis, neuro-fibromatosis, atherosclerosis,         pulmonary fibrosis, arthritis, psoriasis, glomerulonephritis,         restenosis following angioplasty or vascular surgery,         hypertrophic scar formation, inflammatory bowel disease,         transplantation rejection, endotoxic shock, and fungal         infections.     -   defective apoptosis-associated conditions, such as cancers         (including but not limited to those types mentioned         hereinabove), viral infections (including but not limited to         herpesvirus, poxvirus, Epstein-Barr virus, Sindbis virus and         adenovirus), prevention of AIDS development in HIV-infected         individuals, autoimmune diseases (including but not limited to         systemic lupus erythematosus, rheumatoid arthritis, psoriasis,         autoimmune mediated glomerulonephritis, inflammatory bowel         disease and autoimmune diabetes mellitus), neurodegenerative         disorders (including but not limited to Alzheimer's disease,         amyotrophic lateral sclerosis, retinitis pigmentosa, Parkinson's         disease, AIDS-related dementia, spinal muscular atrophy and         cerebellar degeneration), myelodysplastic syndromes, aplastic         anemia, ischemic injury associated with myocardial infarctions,         stroke and reperfusion injury, arrhythmia, atherosclerosis,         toxin-induced or alcohol related liver diseases, hematological         diseases (including but not limited to chronic anemia and         aplastic anemia), degenerative diseases of the musculoskeletal         system (including but not limited to osteroporosis and         arthritis), aspirin-sensitive rhinosinusitis, cystic fibrosis,         multiple sclerosis, kidney diseases and cancer pain.     -   genetic diseases due to mutations in Wnt signaling components,         such as polyposis coli, osteoporosis-pseudoglioma syndrome,         familial exudative vitreoretinopathy, retinal angiogenesis,         early coronary disease, tetra-amelia syndrome, Müllerian-duct         regression and virilization, SERKAL syndrome, diabetes mellitus         type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel         phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity,         split-hand/foot malformation, caudal duplication syndrome, tooth         agenesis, Wilms tumor, skeletal dysplasia, focal dermal         hypoplasia, autosomal recessive anonychia, neural tube defects,         alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF         syndrome, Angelman syndrome, Prader-Willi syndrome,         Beckwith-Wiedemann Syndrome and Rett syndrome.

The compounds and compositions may also be useful in the inhibition of the development of invasive cancer, tumor angiogenesis and metastasis.

Moreover, the compounds and compositions, for example, as inhibitors of the CDKs, can modulate the level of cellular RNA and DNA synthesis and therefore are expected to be useful in the treatment of viral infections such as HIV, human papilloma virus, herpes virus, Epstein-Barr virus, adenovirus, Sindbis virus, pox virus and the like.

Compounds and compositions described herein can inhibit the kinase activity of, for example, CDK/cyclin complexes, such as those active in the G₀. or G.₁ stage of the cell cycle, e.g., CDK2, CDK4, and/or CDK6 complexes.

Evaluation of Biological Activity

The biological activity of the compounds described herein can be tested using any suitable assay known to those of skill in the art, e.g., WO 2001/053268 or WO 2005/009997. For example, the activity of a compound may be tested using one or more of the test methods outlined below.

In one example, tumor cells may be screened for Wnt independent growth. In such a method, tumor cells of interest are contacted with a compound (i.e. inhibitor) of interest, and the proliferation of the cells, e.g. by uptake of tritiated thymidine, is monitored. In some embodiments, tumor cells may be isolated from a candidate patient who has been screened for the presence of a cancer that is associated with a mutation in the Wnt signaling pathway. Candidate cancers include, without limitation, those listed above.

In another example, one may utilize in vitro assays for Wnt biological activity, e.g. stabilization of β-catenin and promoting growth of stem cells. Assays for biological activity of Wnt include stabilization of β-catenin, which can be measured, for example, by serial dilutions of a candidate inhibitor composition. An exemplary assay for Wnt biological activity contacts a Wnt composition in the presence of a candidate inhibitor with cells, e.g. mouse L cells. The cells are cultured for a period of time sufficient to stabilize β-catenin, usually at least about 1 hour, and lysed. The cell lysate is resolved by SDS PAGE, then transferred to nitrocellulose and probed with antibodies specific for β-catenin.

In a further example, the activity of a candidate compound can be measured in a Xenopus secondary axis bioassay (Leyns, L. et al. Cell (1997), 88(6), 747-756).

Example 2

Another screening assay for Wnt activity is described as follows. Reporter cell lines can be generated by stably transducing cells of cancer cell lines (e.g., colon cancer) with a lentiviral construct that include a wnt-responsive promoter driving expression of the firefly luciferase gene.

Lentiviral constructs can be made in which the SP5 promoter, a promoter having eight TCF/LEF binding sites derived from the SP5 promoter, is linked upstream of the firefly luciferase gene. The lentiviral constructs can also include a hygromycin resistance gene as a selectable marker. The SP5 promoter construct can be used to transduce SW480 cells, a colon cancer cell line having a mutated APC gene that generates a truncated APC protein, leading to de-regulated accumulation of β-catenin. A control cell line can be generated using another lentiviral construct containing the luciferase gene under the control of the SV40 promoter which does not require β-catenin for activation.

Cultured SW480 cells bearing a reporter construct can be distributed at approximately 10,000 cells per well into 384 well multiwell plates. Compounds from a small molecule compound library can then be added to the wells in half-log dilutions using a three micromolar top concentration. A series of control wells for each cell type receive only buffer and compound solvent. Twenty-four hours after the addition of compound, reporter activity for luciferases can be assayed, for example, by addition of the BrightGlo luminescence reagent (Promega) and the Victor3 plate reader (Perkin Elmer). Readings can be normalized to DMSO only treated cells, and normalized activities can then be used in the IC₅₀ calculations. Table 2 shows the activity of selected indazole analogs.

TABLE 2 Compound Wnt inhibition, IC₅₀ 1 >10 μM 2 >10 μM 3 >10 μM 4 29-50 nM 11 4 nM 12 26-35 nM 15 5.6 nM 16 0.38-1.17 μM 17 32-50 nM 18 21-39 nM 19 86-206 nM 20 63 nM 21 29 nM 23 34-64 nM

The term “comprising” as used herein is synonymous with “including,” “containing,” or “characterized by,” and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps. 

1. (canceled)
 2. A method of treating a bone or cartilage disease in a subject, the method comprising administering to the subject a therapeutically effective amount of a compound of Formula Ia, or a pharmaceutically acceptable salt thereof:

wherein: R¹, R², R⁴, R⁶, R⁷, R⁸ and R⁹ are independently selected from the group consisting of H, C₁₋₁₉ alkyl, halide, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰, and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰; R³ is selected from the group consisting of —NRS(═O)R¹⁴, —(C₁₋₉ alkyl)R¹⁴, -carbocyclylR¹⁴R¹⁵, -heterocyclylR¹⁴R¹⁵, -arylR¹⁴R¹⁵, and -heteroarylR¹⁴R¹⁵; alternatively, one of each of R¹ and R², R² and R³, R³ and R⁴, R⁶ and R⁷, R⁷ and R⁸ or R⁸ and R⁹ are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl.

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond; each R¹⁰ is independently selected from the group consisting of H, —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl, and —(C₁₋₉ alkyl)_(n)heteroaryl; each R¹¹ is independently selected from the group consisting of —C₁₋₉ alkyl, —CF₃, —(C₁₋₉ alkyl)_(n)carbocyclyl, —(C₁₋₉ alkyl)_(n)heterocyclyl, —(C₁₋₉ alkyl)_(n)aryl, and —(C₁₋₉ alkyl)_(n)heteroaryl; each R¹² is independently selected from the group consisting of —OR¹⁰ and R¹⁰; each R¹³ is 1-5 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclyl, heterocyclyl, aryl, heteroaryl, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰, and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰; R¹⁴ is selected from the group consisting of —NR¹⁰C(=A)R¹⁰, —NR¹⁰S(═O)R¹¹, —NR¹⁰SO₂R¹⁰, —NR¹⁰C(═O)N(R¹⁶)₂, —NR¹⁰C(═S)N(R¹⁰)₂, —NR¹⁰C(═NR²)N(R¹⁰)₂, —N(R¹⁶)₂, —C(═O)NR¹⁰R¹⁷, —C(═S)N(R¹⁰)₂, —C(═NR²)N(R¹⁰)₂, —OC(=A)R¹⁰, —C(=A)R¹⁰, —NR¹⁰C(=A)OR¹⁰, and —OC(=A)NR¹⁰R¹⁰; R¹⁵ is 1-4 substituents each selected from the group consisting of H, C₁₋₉ alkyl, halide, —CF₃, carbocyclylR¹³, heterocyclylR¹³, arylR¹³, heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰, and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰; R¹⁶ is —C₁₋₉ alkyl; each R¹⁷ is independently selected from the group consisting of -heterocyclylR¹³, —(C₁₋₉ alkyl)heterocyclylR¹³, and —(C₁₋₉ alkyl)carbocyclylR¹³; R¹⁸ and R¹⁹ are independently selected from the group consisting of H, C₁₋₉ alkyl, halide, —(C₁₋₉ alkyl)_(n)carbocyclylR¹³, —(C₁₋₉ alkyl)_(n)heterocyclylR¹³, —(C₁₋₉ alkyl)_(n)arylR¹³, —(C₁₋₉ alkyl)_(n)heteroarylR¹³, —(C₁₋₉ alkyl)_(n)OR¹⁰, —(C₁₋₉ alkyl)_(n)SR¹⁰, —(C₁₋₉ alkyl)_(n)S(═O)R¹¹, —(C₁₋₉ alkyl)_(n)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)N(R¹⁰)SO₂R¹⁰, —(C₁₋₉ alkyl)_(n)SO₂N(RO)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)C(=A)N(R¹⁰)₂, —(C₁₋₉ alkyl)_(n)N(R¹⁰)C(=A)R¹⁰, —NO₂, —CN, —(C₁₋₉ alkyl)_(n)CO₂R¹⁰, and —(C₁₋₉ alkyl)_(n)C(=A)R¹⁰; alternatively, R¹⁸ and R¹⁹ are taken together to form a ring which is selected from the group consisting of benzene and pyridine; each A is independently selected from O, S, and NR¹²; Y¹, Y², and Y⁴ are C; Y³ is nitrogen and R⁸ is absent; and each n is 0 or
 1. 3. The method of claim 2, wherein n is
 0. 4. The method of claim 2, wherein n is
 1. 5. The method of claim 2, wherein A is O.
 6. The method of claim 2, wherein R¹, R² and R⁴ are H and R³ is independently selected from the group consisting of —NRS(═O)R¹⁴, —(C₁₋₉alkyl)R¹⁴, -carbocyclylR¹⁴R¹⁵, -heterocyclylR¹⁴R¹⁵, -arylR¹⁴R¹⁵ and -heteroarylR¹⁴R¹⁵.
 7. The method of claim 6, wherein R³ is —(C₁₋₉alkyl)R¹⁴.
 8. The method of claim 6, wherein R³ is -carbocyclylR¹⁴R¹⁵.
 9. The method of claim 6, wherein R³ is -heterocyclylR¹⁴R¹⁶.
 10. The method of claim 6, wherein R³ is -arylR¹⁴R¹⁵.
 11. The method of claim 6, wherein R³ is -heteroarylR¹⁴R¹⁵.
 12. The method of claim 11, wherein R¹⁴ is —NR¹⁰C(=A)R¹⁰ and A is O.
 13. The method of claim 11, wherein R¹⁴ is —C(═O)NR¹⁰R¹⁷.
 14. The method of claim 11, in which the heteroaryl is a pyridine.
 15. The method of claim 11, in which R¹⁴ is —NHC(═O)R¹⁰ and R¹⁰ is selected from the group consisting of —C₁₋₉ alkyl, carbocyclyl, aryl and —(C₁₋₉ alkyl)aryl.
 16. The method of claim 11, in which R¹⁴ is —C(═O)NHR¹⁷, R¹⁷ is —(C₁₋₉ alkyl)carbocyclylR¹³ and R¹³ is H.
 17. The method of claim 2, wherein R⁶ is —(C₁₋₉ alkyl)_(n)heteroarylR¹³, n is 0 and R¹³ is H.
 18. The method of claim 2, wherein R¹, R², R⁴, R⁷, and R⁹ are H; R³ is heteroarylR¹⁴R¹⁵; and R⁶ is —(C₁₋₉ alkyl)_(n)arylR¹³.
 19. The method of claim 18, wherein R¹³ is halide.
 20. The method of claim 19, wherein the halide is fluoro.
 21. The method of claim 2, wherein the bone or cartilage disease is osteoarthritis.
 22. The method of claim 2, wherein the bone or cartilage disease is osteochondrodysplasia.
 23. The method of any of claim 2, wherein the subject is a human.
 24. The method of any of claim 2, wherein the subject is a non-human mammal. 